Research Analyst

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively
• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborate with investigators and site staff to facilitate smooth study conduct
• Perform data review and resolution of queries to maintain high-quality clinical data
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Clinical Research Associate – Sponsor Dedicated

• As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.
• You will build and maintain relationships with clinical sites and investigators.
• Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.
• Responsibilities will include conducting and reporting all types of onsite monitoring visits, driving the study startup phase, performing CRF reviews, source document verification and query resolution.

Senior Clinical Research Associate

• Perform site management activities to ensure compliance with the protocol, monitoring plan, ICH GCP, local regulatory requirements, and sponsor SOPs
• Conduct site qualification, initiation, interim, and close-out visits, both on-site and remotely
• Partner with Clinical Trial Liaison (CTL) and other sponsor functions to support site activation and deliverables
• Establish and maintain productive professional relationships with investigator site staff
• Perform drug accountability, reconciliation, and destruction, ensuring protocol compliance
• Prepare and maintain Oversight Monitoring Plan
• Conduct Oversight Monitoring Visits at sites
• Review and report on status of study conduct at the investigator site
• Ensure site regulatory files are current and timely submission of study documentation
• Identify and record protocol deviations, escalate non-compliance, and resolve study-related issues
• Maintain ongoing communication with site personnel, study teams, and other stakeholders
• Support inspection readiness activities and ensure data integrity and protocol deliverables

Senior Clinical Research Associate – FSP

• Contributes to the selection of potential investigators
• In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance
• Trains, supports, and advises Investigators and site staff in study related matters
• Ensures the sites are inspection ready at all times
• Actively participates in Local Study Team (LST) meetings
• Drives performance at the sites
• Updates CTMS and other systems with data from study sites as per required timelines
• Performs monitoring visits (remote and onsite)
• Ensures data query resolution in a timely manner
• Supports/participates in regular QC checks performed by LSAD or delegate
• Ensures compliance with client ’s Code of Ethics, company policies and procedures

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Clinical Research Associate – Sponsor Dedicated

Senior Clinical Research Associate

Senior Clinical Research Associate – FSP

Clinical Research Associate – FSP